Table 3.
Advantages | Disadvantages | Library amplification | Sequencing technology | |
---|---|---|---|---|
Illumina Inc. | Large user base platform Low cost per base High coverage (high output) | Short reads | Bridge-PCR on flow cell surface | Reversible terminator sequencing by synthesis |
Pacific Biosciences Inc | Very long reads (> 1 kb) Short run time Low reagents cost | High basal error rate Low output | NA | Single-molecule, real-time DNA sequencing by synthesis |
Life Technologies Corp. | High coverage Longer reads | Lower output | PCR on FlowChip surface | Polymerase synthesis |
Sequencing by Oligo Ligation Detection | Low cost per base Low reagents cost Inherent error correction (two-base encoding) | Short reads Long run time | Emulsion PCR | Sequencing by ligation |
Roche Inc. | Longer reads Short run times High coverage | Higher cost per base High reagents cost High error rates in homopolymer repeats | Emulsion PCR on microbeads | Pyrosequencing |
Oxford Nanopore | Very long reads Customization | High error rate Difficult to design multiple parallel pores | NA | Nanopore exonuclease sequencing |
Basic advantages and disadvantages of different sequencing platforms and the sequencing technology or chemistry they use. NA means not applicable.